Canonical Allele Identifier: CA2777662083

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120810608_120810609insAGT , CM000669.2:g.120810608_120810609insAGT	GRCh38
NC_000007.13:g.120450662_120450663insAGT , CM000669.1:g.120450662_120450663insAGT	GRCh37
NC_000007.12:g.120237898_120237899insAGT	NCBI36
NG_023203.1:g.52515_52516insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.361-39_361-38insACT MANE Select	ENSP00000222747.3:n.361-39_361-38insACT
ENST00000222747.7:c.361-39_361-38insACT	ENSP00000222747.3:n.361-39_361-38insACT
ENST00000415871.5:c.361-39_361-38insACT	ENSP00000397699.1:n.361-39_361-38insACT
ENST00000441017.5:c.361-39_361-38insACT	ENSP00000411158.1:n.361-39_361-38insACT
ENST00000450414.5:c.340-39_340-38insACT	ENSP00000397411.1:n.340-39_340-38insACT
NM_012338.3:c.361-39_361-38insACT	NP_036470.1:n.361-39_361-38insACT
XM_005250239.1:c.361-39_361-38insACT	XP_005250296.1:n.361-39_361-38insACT
XM_011515993.1:c.361-39_361-38insACT	XP_011514295.1:n.361-39_361-38insACT
XM_011515994.1:c.361-39_361-38insACT	XP_011514296.1:n.361-39_361-38insACT
XM_005250239.3:c.361-39_361-38insACT	XP_005250296.1:n.361-39_361-38insACT
XM_017011913.1:c.286-39_286-38insACT	XP_016867402.1:n.286-39_286-38insACT
NM_012338.4:c.361-39_361-38insACT MANE Select	NP_036470.1:n.361-39_361-38insACT